Chapter 7-Genetic Mutations and Biotechnology
The number of chromosomes can be studied by looking at a _____.
Karyotype
The genetic disorder that causes a male to be born with two X chromosomes in addition to a Y chromosome so they have XXY instead of XY is called _____.
Klinefelter syndrome
Making changes in an organism's DNA is called _____.
Genetic engineering
All of an organisms hereditary information is called a _____.
Genome
Sickle cell disease is a genetic disorder that affects hemoglobin. In the gene that coded for hemoglobin, the normal condon sequence GAG becomes GUG, and as a result, the amino acid glutamine is replaced with valine. What type of mutation causes sickle cell disease?
Point
A frame shift mutation is usually more serious than a substitution mutation because it changes every _____ after the mutation.
Condon
Insertion and deletion mutations are usually more serious than substitution because they change every _____ after the mutation.
Condon
A danger of creating transgenic organisms is that they may _____ the gene pool of organisms that are not transgenic.
Contaminate
The genetic disorder caused when a child is born with three copies of chromosome 21 instead of two is called _____.
Down syndrome
Two ethical concerns raised by the Human Genome Project are the potential for _____ and an individuals right to _____ regarding their health.
Discrimination, privacy
A doctor suspects a person may have Klinefelter's syndrome (XXY) caused by having an extra X chromosome. Which of the following would be best to confirm the diagnosis?
Karyotype
Turner syndrome is a chromosomal mutation resulting from nondisjunction during meiosis in forming either sperm or egg cells. Which genetic technology would be best to determine the presence of this chromosomal mutation?
Karyotype
A mutation can be passed to offspring only when the mutation is present or occurs during _____.
Meiosis
An agent that can cause a change in DNA is called a _____.
Mutagen
The failure of paired chromosomes to separate properly during meiosis is called _____.
Nondisjunction
_____ during meiosis is responsible for down syndrome
Nondisjunction
Using electrophoresis to analyze DNA allows researchers to find differences and similarities in different kinds of _____.
Organisms
Organisms that contain genes from a different organism are called _____.
Transgenic
To make potatoes more tolerant of cold storage, genetic engineers inserted codfish genes into a potato plant. Since these potato plants contain DNA from another organism, how are they classified?
Transgenic
A _____ is an organism that contains genes from a different species.
Transgenic organism
_____ is a mutation where part of a chromosome breaks off and attaches to a non-homologous pair.
Translocation
Having three of a particular chromosome instead of two is called _____.
Trisomy
_____ is where a person has a missing enzyme needed to destroy a certain type of fat on the brain. Babies usually appear normal around 3 months old.
Tay-Sachs disease
_____ has been used to produce insulin for diabetes treatment.
Bacterial transformation
The process of producing genetically identical copies of genes, tissues, or an entire organism is called _____.
Cloning
A point mutation that occurs in a blood cell would most likely result in incorrect _____ for a protein.
Coding
_____ is caused by a defective transport protein that carries salt and water into and out of the cells in the lungs.
Cystic fibrosis
A mutation is any mistake or change in the _____.
DNA
DNA fingerprint helps to identify a person because not two people, except identical twins, have exactly the same _____.
DNA
Transformation is the process of placing _____ from one organism into another organism.
DNA
_____ is a unique pattern created from DNA segments that can be used to identify family relationships.
DNA fingerprint
A piece of a chromosome breaks off describes _____.
Deletion
The main ethical concern behind stem cell research is that some research uses embryos that are _____ when harvesting the cells.
Destroyed
Transgenic organisms are produced when the genes from one species are inserted into the genome of another species. For example, bt corn contains genes from the bacteria Bacillus Thuringiensis that makes the corn plant toxic to corn-borer caterpillars. The primary ethical concern of growing transgenic plants such as bt-corn are the unforeseen consequences on the _____ and _____.
Environment, human health
A substitution mutation results in the formation of a stop condon in the middle of a gene sequence. This mutation will affect the protein being formed by making the protein contain _____ amino acids than it should.
Fewer
Gel electrophoresis can be used to separate DNA fragments by charge and length to create a DNA _____.
Fingerprint
_____ is an error in a DNA sequence that adds or deleted a single base.
Frameshift
It would be best to use _____ to compare the banding patterns when trying to determine any taxonomic relationship between two organisms that have similar appearance and are found within a similar environment.
Gel electrophoresis
Several new organisms were recently discovered in the same environment. You could best determine if he organisms are related by comparing the DNA or organisms through _____.
Gel electrophoresis
Small pieces of DNA are separated into segments of different length during the process of _____.
Gel electrophoresis
Using _____ to create DNA fingerprints would be the best technology to determine if two people are related.
Gel electrophoresis
_____ is a laboratory technique that runs an electrical current through a gel to separate DNA fragments by their size.
Gel electrophoresis
_____ is a sex linked trait where the person's blood does not clot normally so the person bleeds more and longer from an injury.
Hemophilia
The _____ is an international effort that successfully sequenced human DNA.
Human genome project
_____ is one of the only disorders caused by a dominant gene. It affects the brain, causing mental illness and death.
Huntington's disease
Cloning produces organisms that are genetically _____ to the original organism.
Identical
The nucleotide sequence on a strand of DNA changes as shown: ATA CGA TCG to ATA CGA TCC G. What type of mutation has occurred?
Insertion
_____ is a mutation where part of a chromosome breaks off and is inserted backwards.
Inversion
_____ is where too much phenylalanine builds up on the brain and it can be controlled with a special diet.
PKU
A circular piece of DNA found in bacterial cells is called _____.
Plasmid
In sickle cell disease, the gene responsible for forming hemoglobin inserts the amino acid valine instead of glutamic acid. Only this one amino acid is affected, but the resulting protein is shaped incorrectly. A _____ mutation causes sickle cell anemia.
Point
Tay-Sachs disease is caused by a frameshift mutation on chromosome 15. A person with this disease lacks the enzyme hexosaminidase A. This enzyme is needed to break down gangliosides, a fatty substance that is formed in nerve cells and in the brain. The frameshift mutation results in this disease because it causes a defect in the gene needed to create a _____.
Protein
_____ is DNA that is formed by joining a short piece of DNA from one organism to the DNA of another organism.
Recombinant DNA
A sex linked trait found more often in males where the person has trouble distinguishing certain colors describes _____.
Red-green color blindness
Cystic fibrosis is most commonly caused when a gene on chromosome 7 is missing three base pairs that code for one amino acid in a protein. You could expect this missing amino acid to affect the protein by making it abnormally _____.
Shaped
A point mutation that causes red blood cells to be a different shape and less functional and makes them sticky is called _____.
Sickle cell anemia
_____ are undifferentiated cells that have the ability to become different types of specialized cells.
Stem cells
An error in the DNA sequence in which one base is misread and changed to a different base is _____.
Substitution
If a doctor suspects down syndrome in a developing fetus, he should observe _____ copies of a certain chromosome with a karyotype.
Three